Nexstim Plc - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Nexstim Plc has 2 FDA 510(k) cleared medical devices. Based in Helsinki, FI.
Historical record: 2 cleared submissions from 2017 to 2019. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Nexstim Plc Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Nexstim Plc
2 devices